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Digital Storytelling in Pediatric Safe Drug

E

Ege University

Status

Completed

Conditions

Education
Innovativeness
Nursing

Treatments

Other: Digital Education Group

Study type

Interventional

Funder types

Other

Identifiers

NCT05845957
Bakircay

Details and patient eligibility

About

Summary Aim: This research was conducted to determine the effectiveness of education given to students using digital storytelling in safe pediatric intravenous drug administration.

Method: It is a randomized controlled experimental study. The sample of the study consisted of 84 nursing students. The students included in the study were divided into two equal groups: the experimental and control groups. Digital education material of the experimental group and theoretical education was applied to the control group. Before and after the training, a post-knowledge test was made and evaluated.

Enrollment

84 patients

Sex

All

Ages

19 to 23 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Being a student of the Department of Nursing
  • Taking the child health and diseases nursing course and being successful
  • Volunteering to participate in the research

Exclusion criteria

  • Participate and quit the study
  • Being a 1st and 2nd year nursing student
  • Failure of the child health and diseases nursing course

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

84 participants in 2 patient groups

Digital Education Group
Experimental group
Description:
All participants in this group were given the "Safe pediatric intravenous drug administration knowledge test" prepared by the researchers as a pre-test. The participants of this group, who were determined by randomization, were given training prepared using the digital storytelling method. The training took 25 minutes. After the training, the "Safe intravenous drug administration knowledge test" was applied as a post-test.
Treatment:
Other: Digital Education Group
Control Group
No Intervention group
Description:
No intervention was made. All participants in this group were given the "Safe pediatric intravenous drug administration knowledge test" prepared by the researchers as a pre-test. Afterward, theoretical information on the subject was given. After theoretical information, the "Safe intravenous drug administration knowledge test" was applied as a post-test.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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